<p>We are in the era of millimetre-scale electron microscopy volumes collected at nanometre resolution<sup><CitationRef CitationID="CR1">1</CitationRef>,<CitationRef CitationID="CR2">2</CitationRef></sup>. Dense reconstruction of cellular compartments in these electron microscopy volumes has been enabled by recent advances in machine learning<sup><CitationRef AdditionalCitationIDS="CR4 CR5" CitationID="CR3">3</CitationRef>–<CitationRef CitationID="CR6">6</CitationRef></sup>. Automated segmentation methods produce exceptionally accurate reconstructions of cells, but post hoc proofreading is still required to generate large connectomes that are free of merge and split errors. The elaborate 3D meshes of neurons in these volumes contain detailed morphological information at multiple scales, from the diameter, shape and branching patterns of axons and dendrites, down to the fine-scale structure of dendritic spines. However, extracting these features can require substantial effort to piece together existing tools into custom workflows. Here, building on existing open source software for mesh manipulation, we present Neural Decomposition (NEURD), a software package that decomposes meshed neurons into compact and extensively annotated graph representations. With these feature-rich graphs, we automate a variety of tasks such as state-of-the-art automated proofreading of merge errors, cell classification, spine detection, axonal-dendritic proximities and other annotations. These features enable many downstream analyses of neural morphology and connectivity, making these massive and complex datasets more accessible to neuroscience researchers.</p>

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NEURD offers automated proofreading and feature extraction for connectomics

  • Brendan Celii,
  • Stelios Papadopoulos,
  • Zhuokun Ding,
  • Paul G. Fahey,
  • Eric Wang,
  • Christos Papadopoulos,
  • Alexander B. Kunin,
  • Saumil Patel,
  • J. Alexander Bae,
  • Agnes L. Bodor,
  • Derrick Brittain,
  • JoAnn Buchanan,
  • Daniel J. Bumbarger,
  • Manuel A. Castro,
  • Erick Cobos,
  • Sven Dorkenwald,
  • Leila Elabbady,
  • Akhilesh Halageri,
  • Zhen Jia,
  • Chris Jordan,
  • Dan Kapner,
  • Nico Kemnitz,
  • Sam Kinn,
  • Kisuk Lee,
  • Kai Li,
  • Ran Lu,
  • Thomas Macrina,
  • Gayathri Mahalingam,
  • Eric Mitchell,
  • Shanka Subhra Mondal,
  • Shang Mu,
  • Barak Nehoran,
  • Sergiy Popovych,
  • Casey M. Schneider-Mizell,
  • William Silversmith,
  • Marc Takeno,
  • Russel Torres,
  • Nicholas L. Turner,
  • William Wong,
  • Jingpeng Wu,
  • Szi-chieh Yu,
  • Wenjing Yin,
  • Daniel Xenes,
  • Lindsey M. Kitchell,
  • Patricia K. Rivlin,
  • Victoria A. Rose,
  • Caitlyn A. Bishop,
  • Brock Wester,
  • Emmanouil Froudarakis,
  • Edgar Y. Walker,
  • Fabian Sinz,
  • H. Sebastian Seung,
  • Forrest Collman,
  • Nuno Maçarico da Costa,
  • R. Clay Reid,
  • Xaq Pitkow,
  • Andreas S. Tolias,
  • Jacob Reimer

摘要

We are in the era of millimetre-scale electron microscopy volumes collected at nanometre resolution1,2. Dense reconstruction of cellular compartments in these electron microscopy volumes has been enabled by recent advances in machine learning36. Automated segmentation methods produce exceptionally accurate reconstructions of cells, but post hoc proofreading is still required to generate large connectomes that are free of merge and split errors. The elaborate 3D meshes of neurons in these volumes contain detailed morphological information at multiple scales, from the diameter, shape and branching patterns of axons and dendrites, down to the fine-scale structure of dendritic spines. However, extracting these features can require substantial effort to piece together existing tools into custom workflows. Here, building on existing open source software for mesh manipulation, we present Neural Decomposition (NEURD), a software package that decomposes meshed neurons into compact and extensively annotated graph representations. With these feature-rich graphs, we automate a variety of tasks such as state-of-the-art automated proofreading of merge errors, cell classification, spine detection, axonal-dendritic proximities and other annotations. These features enable many downstream analyses of neural morphology and connectivity, making these massive and complex datasets more accessible to neuroscience researchers.